The First Department of Internal Medicine, Yokohama City University, School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama 236, Japan.
Environ Toxicol Pharmacol. 1996 Aug 15;2(1):25-30. doi: 10.1016/1382-6689(96)00024-5.
To evaluate the involvement of superoxide in ozone (O(3))-induced airway hyperresponsiveness, we studied the effects of superoxide dismutase (SOD), a scavenger of superoxide anion, and apocynin, an inhibitor of superoxide anion-generating NADPH oxidase in phagocytes, on the airway responses induced by O(3) in unanesthetized guinea pigs. Airway responsiveness was measured by PC(200)Mch, the concentration required to produce a doubling in the baseline specific airway resistance to an inhaled methacholine aerosol, in spontaneously breathing animals. Before exposure to 3 ppm O(3) for 30 min, animals inhaled either SOD (5000 U/ml) or vehicle for 5 min. Although SOD did not affect PC(200)Mch in the air control group, this agent reduced the O(3)-induced airway hyperresponsiveness. Repeated administration of apocynin (12 mg/kg for 4 days) also attenuated the O(3)-induced airway hyperresponsiveness. These data suggest that superoxide may be involved in the pathogenesis of O(3)-induced airway hyperresponsiveness, possibly through the stimulation of superoxide anions release from bronchoalveolar phagocytes. The data also suggest a potential therapeutic role for antioxidants in oxidant injury by air pollutants.
为了评估超氧阴离子自由基在臭氧(O3)诱导的气道高反应性中的作用,我们研究了超氧化物歧化酶(SOD)——一种超氧阴离子自由基清除剂,以及脱镁叶绿酸 a,一种吞噬细胞中超氧阴离子生成 NADPH 氧化酶的抑制剂,对未麻醉豚鼠 O3 诱导的气道反应的影响。气道反应性通过 PC200Mch 来测量,即在吸入乙酰甲胆碱气溶胶时,引起基础特异性气道阻力增加一倍所需的浓度。在暴露于 3ppm O3 30 分钟之前,动物吸入 SOD(5000U/ml)或载体 5 分钟。尽管 SOD 对空气对照组的 PC200Mch 没有影响,但该药物可降低 O3 诱导的气道高反应性。重复给予脱镁叶绿酸 a(4 天内 12mg/kg)也可减轻 O3 诱导的气道高反应性。这些数据表明,超氧阴离子自由基可能参与了 O3 诱导的气道高反应性的发病机制,可能是通过刺激支气管肺泡吞噬细胞中超氧阴离子自由基的释放。这些数据还表明,抗氧化剂在空气污染物引起的氧化损伤中可能具有潜在的治疗作用。